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									<identifier>oai:www.peertechzpublications.org:10.17352/ac.000008</identifier>
									<datestamp>2017-07-03</datestamp>
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										<dc:title>
										Fever Induced Brugada Syndrome
										</dc:title><dc:creator>Aditya A Munshi</dc:creator><dc:description>&lt;p&gt;Brugada syndrome is a heterogeneous genetic channelopathy that predisposes to ventricular arrhythmias and sudden cardiac death (SCD). The electrocardiogram (ECG) findings only suggest a diagnosis of Brugada syndrome but are not confirmatory. The ECG pattern is known to vary with time in some patients and many have a normal baseline ECG [1,2]. There are two distinctly described ECG patterns, type I Brugada is characterized by ST elevation (≥2mm) with a “coved” pattern or a T-wave which is inverted with an upward convexity, in other cases the elevated ST segment descends and rises again forming a “saddleback” type pattern, this is called the type II Brugada. The electrophysiological and clinical manifestations of this syndrome have been found to be secondary to various factors [3-10]. Of these, mutations in cardiac sodium channel SCN genes (SCN5A and SCN10A) are the most well-known [11]. Since all affected families do not have these mutations, it is believed that other mutations in sodium channel genes or mutations in non-sodium channel genes may also cause Brugada syndrome [12-15].&lt;/p&gt;</dc:description>
										<dc:publisher>Annals of Circulation - Peertechz Publications</dc:publisher>
										<dc:date>2017-07-03</dc:date>
										<dc:type>Letter to Editor</dc:type>
										<dc:identifier>https://doi.org/10.17352/ac.000008</dc:identifier>
										<dc:language>en</dc:language>
										<dc:rights>Copyright © Aditya A Munshi et al.</dc:rights>
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